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Study Site Management Specialist(m/w/x)
As a Site Activation Lead, you will drive the start-up of clinical trials by aligning with client goals and managing site activation plans. Your role involves overseeing project delivery, ensuring compliance, and leading key communications to achieve successful outcomes.
Anforderungen
- Bachelor’s Degree in life sciences
- Minimum of 5 years of experience in Clinical Research
- Strong project management skills
- Excellent written and verbal communication abilities
- Proven ability to work efficiently to tight deadlines
Aufgaben
- Lead clinical trial start-up activities
- Understand client objectives and develop site distribution plans
- Oversee daily site activation delivery for assigned projects
- Ensure compliance with sponsor timelines and ICON/client KPIs
- Create comprehensive site activation plans for each project
- Conduct kick-off meetings and project updates
- Facilitate bid defenses and status calls
- Utilize project management skills to enhance collaboration
Berufserfahrung
Ausbildung
Sprachen
Benefits
Mehr Urlaubstage
- •Various annual leave entitlements
Gesundheits- & Fitnessangebote
- •Health insurance offerings
Betriebliche Altersvorsorge
- •Retirement planning offerings
Mentale Gesundheitsförderung
- •Global Employee Assistance Programme
Sonstige Vorteile
- •Life assurance
Sonstige Zulagen
- •Flexible optional benefits
- 176 ICON Clinical Research Germany GmbHVollzeitmit HomeofficeSeniorMannheim
- ICON Clinical Research Germany GmbH
Clinical Trial Assistant (CTA)(m/w/x)
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Study Site Management Specialist(m/w/x)
As a Site Activation Lead, you will drive the start-up of clinical trials by aligning with client goals and managing site activation plans. Your role involves overseeing project delivery, ensuring compliance, and leading key communications to achieve successful outcomes.
Anforderungen
- Bachelor’s Degree in life sciences
- Minimum of 5 years of experience in Clinical Research
- Strong project management skills
- Excellent written and verbal communication abilities
- Proven ability to work efficiently to tight deadlines
Aufgaben
- Lead clinical trial start-up activities
- Understand client objectives and develop site distribution plans
- Oversee daily site activation delivery for assigned projects
- Ensure compliance with sponsor timelines and ICON/client KPIs
- Create comprehensive site activation plans for each project
- Conduct kick-off meetings and project updates
- Facilitate bid defenses and status calls
- Utilize project management skills to enhance collaboration
Berufserfahrung
Ausbildung
Sprachen
Benefits
Mehr Urlaubstage
- •Various annual leave entitlements
Gesundheits- & Fitnessangebote
- •Health insurance offerings
Betriebliche Altersvorsorge
- •Retirement planning offerings
Mentale Gesundheitsförderung
- •Global Employee Assistance Programme
Sonstige Vorteile
- •Life assurance
Sonstige Zulagen
- •Flexible optional benefits
Über das Unternehmen
176 ICON Clinical Research Germany GmbH
Branche
Healthcare
Beschreibung
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on innovative treatments.
- 176 ICON Clinical Research Germany GmbH
Senior Clinical Research Associate(m/w/x)
Vollzeitmit HomeofficeSeniorMannheim - ICON Clinical Research Germany GmbH
Clinical Trial Assistant (CTA)(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenMannheim - Penumbra
Clinical Specialist(m/w/x)
Vollzeitmit HomeofficeSeniorWürzburg, Erlangen, Nürnberg, Mannheim, Stuttgart - The Binding Site GmbH
Senior Account Manager – Diagnostics Sales(m/w/x)
VollzeitRemoteSeniorHamburg, Schwetzingen - Deutsche Krebsforschungszentrum
Projektmanager:innen in der klinischen Forschung(m/w/x)
Vollzeit/TeilzeitBefristeter Vertragmit HomeofficeJuniorHeidelberg